Technical Field
[0001] The present invention relates to low yield ratio, high strength and high uniform
elongation steel plates suitable for use mainly in line pipes and methods for manufacturing
the same and particularly relates to a low yield ratio, high strength and high uniform
elongation steel plate having excellent strain ageing resistance and a method for
manufacturing the same. The term "uniform elongation" as used herein is also called
even elongation and refers to the limit of the permanent elongation of a parallel
portion of a specimen uniformly deformed in a tensile test. The uniform elongation
is usually determined in the form of the permanent elongation corresponding to the
maximum tensile load.
Background Art
[0002] In recent years, steels for welded structures have been required to have low yield
strength and high uniform elongation in addition to high strength and high toughness
from the viewpoint of earthquake-proof. For example, steels for line pipes used in
quake zones which may possibly be deformed significantly are required to have low
yield strength and high uniform elongation in some cases. In general, it is known
that the yield strength and uniform elongation of steel can be reduced and increased,
respectively, in such a manner that the metallographic microstructure of the steel
is transformed into a microstructure in which a hard phase such as bainite or martensite
is adequately dispersed in ferrite, which is a soft phase.
[0003] As for manufacturing methods capable of obtaining a microstructure in which a hard
phase is adequately dispersed in a soft phase as described above, Patent Literature
1 discloses a heat treatment method in which quenching (Q') from the two-phase (γ
+ α) temperature range of ferrite and austenite is performed between quenching (Q)
and tempering (T).
[0004] As for methods in which the number of manufacturing steps is not increased, Patent
Literature 2 discloses a method in which after rolling is finished at the Ar
3 transformation temperature or higher, the start of accelerated cooling is delayed
until the temperature of a steel material decreases to the Ar
3 transformation temperature, at which ferrite is produced, or lower.
[0005] As for techniques for achieving low yield ratio without performing such heat treatment
as disclosed in Patent Literature 1 or 2, Patent Literature 3 discloses a method in
which low yield ratio is achieved in such a manner that after the rolling of a steel
material is finished at the Ar
3 transformation temperature or higher, the rate of accelerated cooling and the finishing
cooling temperature are controlled such that a two-phase microstructure consisting
of acicular ferrite and martensite is produced.
[0006] Furthermore, as for techniques for achieving low yield ratio and excellent welded
heat affected zone toughness without significantly increasing the amount of an alloying
element added to steel, Patent Literature 4 discloses a method in which a three-phase
microstructure consisting of ferrite, bainite, and island martensite (M-A constituent)
is produced in such a manner that Ti/N and/or the Ca-O-S balance is controlled.
[0007] Patent Literature 5 discloses a technique in which low yield ratio and high uniform
elongation are achieved by the addition of an alloying element such as Cu, Ni, or
Mo.
[0008] On the other hand, welded steel pipes, such as UOE steel pipes and electric welded
pipes, used for line pipes are manufactured in such a manner that steel plates are
cold-formed into pipes, abutting surfaces thereof are welded, and the outer surfaces
of the pipes are usually subjected to coating such as polyethylene coating or powder
epoxy coating from the viewpoint of corrosion resistance. Therefore, there is a problem
in that the steel pipes have a yield ratio greater than the yield ratio of the steel
plates because strain ageing is caused by working strain during pipe making and heating
during coating and the yield stress is increased. In order to cope with such a problem,
for example, Patent Literatures 6 and 7 each disclose a steel pipe which has excellent
strain ageing resistance, low yield ratio, high strength, and high toughness and which
contains fine precipitates of composite carbides containing Ti and Mo or fine precipitates
of composite carbides containing two or more of Ti, Nb, and V and also disclose a
method for manufacturing the steel pipe.
Citation List
Patent Literature
[0009]
PTL 1: Japanese Unexamined Patent Application Publication No. 55-97425
PTL 2: Japanese Unexamined Patent Application Publication No. 55-41927
PTL 3: Japanese Unexamined Patent Application Publication No. 1-176027
PTL 4: Japanese Patent No. 4066905 (Japanese Unexamined Patent Application Publication No. 2005-48224)
PTL 5: Japanese Unexamined Patent Application Publication No. 2008-248328
PTL 6: Japanese Unexamined Patent Application Publication No. 2005-60839
PTL 7: Japanese Unexamined Patent Application Publication No. 2005-60840
Summary of Invention
Technical Problem
[0010] The heat treatment method disclosed in Patent Literature 1 is capable of achieving
low yield ratio by appropriately selecting the quenching temperature of the two-phase
(γ + α) temperature range and, however, includes an increased number of heat treatment
steps. Therefore, there is a problem in that a reduction in productivity and an increase
in manufacturing cost are caused.
[0011] In the technique disclosed in Patent Literature 2, cooling needs to be performed
at a cooling rate close to a natural cooling rate in the temperature range from the
end of rolling to the start of accelerated cooling. Therefore, there is a problem
in that productivity is extremely low.
[0012] In the technique disclosed in Patent Literature 3, in order to allow a steel material
to have a tensile strength of 490 N/mm
2 (50 kg/mm
2) or more as described in an example, the steel material needs to have an increased
carbon content or a composition in which the amount of an added alloying element is
increased, which causes an increase in material cost and a problem in that the toughness
of a welded heat affected zone is deteriorated.
[0013] In the technique disclosed in Patent Literature 4, the influence of a microstructure
on uniform elongation performance required for pipelines has not necessarily become
clear.
[0014] In the technique disclosed in Patent Literature 5, a composition in which the amount
of an added alloying element is increased is required, which causes an increase in
material cost and a problem in that the toughness of a welded heat affected zone is
deteriorated.
[0015] In the technique disclosed in Patent Literature 6 or 7, strain ageing resistance
is improved; however, it remains unsolved that strain ageing resistance and uniform
elongation performance required for pipelines are both ensured.
In Patent Literatures 1 to 7, a ferrite phase is essential. When the ferrite phase
is contained, an increase in strength to X60 or higher in API standards causes a reduction
in tensile strength and the amount of an alloying element needs to be increased in
order to ensure strength, which may possibly cause an increase in alloying cost and
a reduction in low-temperature toughness.
[0016] As described above, it is difficult for the conventional techniques to manufacture
low yield ratio, high strength and high uniform elongation steel plates having excellent
welded heat affected zone toughness, high uniform elongation, and excellent strain
ageing resistance without causing a reduction in productivity or an increase in manufacturing
cost.
[0017] Therefore, it is an object of the present invention to provide a low yield ratio,
high strength and high uniform elongation steel plate and a method for manufacturing
the same. The low yield ratio, high strength and high uniform elongation steel plate
is capable of solving such problems with the conventional techniques, can be manufactured
at high efficiency and low cost, and has high uniform elongation equivalent to API
5L X60 Grade or higher (herein, particularly X65 and X70 Grades).
Solution to Problem
[0018] In order to solve the above problems, the inventors have intensively investigated
methods for manufacturing steel plates, particularly manufacturing processes including
controlled rolling, accelerated cooling subsequent to controlled rolling, and reheating
subsequent thereto. As a result, the inventors have obtained findings below.
[0019]
- (a) Cooling is stopped in a temperature range in which non-transformed austenite is
present, that is, during bainite transformation, in the course of accelerated cooling
and reheating is started at a temperature higher than the bainite transformation finish
temperature (hereinafter referred to as the Bf point), whereby the metallographic
microstructure of a steel plate is transformed into a two phase microstructure in
which hard M-A constituent (hereinafter referred to as MA) is uniformly produced and
bainite and low yield ratio can be achieved.
[0020] MA can be readily identified in such a manner that a steel plate is etched with,
for example, 3% nital (a solution of nitric acid in alcohol), is subjected to electrolytic
etching, and is then observed. MA is observed as a white prominent portion when the
microstructure of the steel plate is observed with a scanning electron microscope
(SEM).
[0021]
(b) Since the addition of appropriate amounts of austenite-stabilizing elements such
as Mn and Si stabilizes non-transformed austenite, hard MA can be produced without
the addition of a large amount of an alloying element such as Cu, Ni, or Mo.
[0022]
(c) MA can be uniformly and finely dispersed and the uniform elongation can be improved
with the yield ratio maintained low by applying an accumulative rolling reduction
of 50% or more in a no-recrystallization temperature range in austenite not higher
than 900°C.
[0023]
(d) Furthermore, the shape of MA can be controlled, that is, MA can be refined to
an average equivalent circle diameter of 3.0 µm or less by adequately controlling
rolling conditions in the no-recrystallization temperature range in austenite described
in Item (c) and the reheating conditions described in Item (a). As a result, the decomposition
of MA is slight even though such a thermal history that causes the deterioration in
yield ratio of conventional steels is suffered; hence, desired structural morphology
and properties can be maintained after ageing.
[0024] The present invention has been made on the basis of the above findings and additional
studies. The scope of the present invention is as described below.
[0025] The first invention provides a low yield ratio, high strength and high uniform elongation
steel plate containing 0.06% to 0.12% C, 0.01% to 1.0% Si, 1.2% to 3.0% Mn, 0.015%
or less P, 0.005% or less S, 0.08% or less Al, 0.005% to 0.07% Nb, 0.005% to 0.025%
Ti, 0.010% or less N, and 0.005% or less O on a mass basis, the remainder being Fe
and unavoidable impurities. The low yield ratio, high strength and high uniform elongation
steel plate has a metallographic microstructure that is a two-phase microstructure
consisting of bainite and M-A constituent, the area fraction of the M-A constituent
being 3% to 20%, the equivalent circle diameter of the M-A constituent being 3.0 µm
or less. The low yield ratio, high strength and high uniform elongation steel plate
has a uniform elongation of 7% or more and a yield ratio of 85% or less. The low yield
ratio, high strength and high uniform elongation steel plate has a uniform elongation
of 7% or more and a yield ratio of 85% or less after being subjected to strain ageing
treatment at a temperature of 250°C or lower for 30 minutes or less.
[0026] The second invention provides the low yield ratio, high strength and high uniform
elongation steel plate, according to the first invention, further containing one or
more selected from the group consisting of 0.5% or less Cu, 1% or less Ni, 0.5% or
less Cr, 0.5% or less Mo, 0.1% or less V, 0.0005% to 0.003% Ca, and 0.005% or less
B on a mass basis.
[0027] The third invention provides a method for manufacturing a low yield ratio, high strength
and high uniform elongation steel plate. The method includes heating steel having
the composition specified in the first or second invention to a temperature of 1000°C
to 1300°C, hot-rolling the steel at a finishing rolling temperature not lower than
the Ar
3 transformation temperature such that the accumulative rolling reduction at 900°C
or lower is 50% or more, performing accelerated cooling to a temperature of 500°C
to 680°C at a cooling rate of 5 °C/s or more, and immediately performing reheating
to a temperature of 550°C to 750°C at a heating rate of 2.0 °C/s or more.
Advantageous Effects of Invention
[0028] According to the present invention, a low yield ratio, high strength and uniform
elongation steel plate having high uniform elongation properties can be manufactured
at low cost without deteriorating the toughness of a welded heat affected zone or
adding a large amount of an alloying element. Therefore, a large number of steel plates
mainly used for line pipes can be stably manufactured at low cost and productivity
and economic efficiency can be significantly increased, which is extremely industrially
advantageous.
Brief Description of Drawings
[0029]
[Fig. 1] Fig. 1 is a graph showing the relationship between the area fraction of MA
and the uniform elongation of base materials.
[Fig. 2] Fig. 2 is a graph showing the relationship between the area fraction of MA
and the yield ratio of base materials.
[Fig. 3] Fig. 3 is a graph showing the relationship between the area fraction of MA
and the toughness of base materials.
Description of Embodiments
[0030] Reasons for limiting requirements of the present invention are described below.
1. Composition
[0031] Reasons for limiting the composition of steel according to the present invention
are first described. The percentages of all components are on a mass basis.
C: 0.06% to 0.12%
[0032] C is an element which contributes to precipitation hardening in the form of carbides
and which is important in producing MA. The addition of less than 0.06% C is insufficient
to produce MA and therefore sufficient strength cannot possibly be ensured. The addition
of more than 0.12% C deteriorates the toughness of a welded heat affected zone (HAZ).
Therefore, the content of C is within the range of 0.06% to 0.12%. The content thereof
is preferably within the range of 0.06% to 0.10%.
Si: 0.01% to 1.0%
[0033] Si is added for deoxidation. The addition of less than 0.01% Si is insufficient to
obtain a deoxidation effect. The addition of more than 1.0% Si causes the deterioration
of toughness and weldability. Therefore, the content of Si is within the range of
0.01% to 1.0%. The content thereof is preferably within the range of 0.1% to 0.3%.
Mn: 1.2% to 3.0%
[0034] Mn is added for the improvement of strength, toughness, and hardenability to promote
the production of MA. The addition of less than 1.2% Mn is insufficient to obtain
such an effect. The addition of more than 3.0% Mn causes the deterioration of toughness
and weldability. Therefore, the content of Mn is within the range of 1.2% to 3.0%.
In order to stably produce MA independently of the variation of components and manufacturing
conditions, the content thereof is preferably 1.5% or more. The content thereof is
more preferably within the range of 1.5% to 1.8%.
P and S: 0.015% or less and 0.005% or less, respectively
[0035] In the present invention, P and S are unavoidable impurities and therefore the upper
limits of the contents thereof are limited. High P content causes significant center
segregation to deteriorate the toughness of the base material; hence, the content
of P is 0.015% or less. High S content causes a significant increase in production
of MnS to deteriorate the toughness of the base material; hence, the content of S
is 0.005% or less. The content of P is preferably 0.010% or less. The content of S
is preferably 0.002% or less.
Al: 0.08% or less
[0036] Al is added as a deoxidizing agent. The addition of less than 0.01% Al is insufficient
to obtain a deoxidation effect. The addition of more than 0.08% Al causes a decrease
in cleanliness and a reduction in toughness of the steel. Therefore, the content of
Al is 0.08% or less. The content thereof is preferably within the range of 0.01% to
0.08% and more preferably 0.01% to 0.05%.
Nb: 0.005% to 0.07%
[0037] Nb is an element which contributes to the increase of toughness due to the refining
of a microstructure and also contributes to the increase of strength due to an increase
in hardenability of solute Nb. Such effects are developed by the addition of 0.005%
or more Nb. However, the addition of less than 0.005% Nb is ineffective. The addition
of more than 0.07% Nb deteriorates the toughness of the welded heat affected zone.
Therefore, the content of Nb is within the range of 0.005% to 0.07%. The content thereof
is preferably within the range of 0.01% to 0.05%.
Ti: 0.005% to 0.025%
[0038] Ti is an important element which suppresses the coarsening of austenite during the
heating of a slab by a pinning effect to increase the toughness of the base material.
Such an effect is developed by the addition of 0.005% or more Ti. However, the addition
of more than 0.025% Ti deteriorates the toughness of the welded heat affected zone.
Therefore, the content of Ti is within the range of 0.005% to 0.025%. From the viewpoint
of the toughness of the welded heat affected zone, the content of Ti is preferably
within the range of 0.005% to less than 0.02% and more preferably 0.007% to 0.016%.
N: 0.010% or less
[0039] N is treated as an unavoidable impurity. When the content of N is more than 0.010%,
the toughness of the welded heat affected zone is deteriorated. Therefore, the content
of N is 0.010% or less. The content thereof is preferably 0.007% or less and more
preferably 0.006% or less.
0: 0.005% or less
[0040] In the present invention, O is an unavoidable impurity and therefore the upper limit
of the content thereof is limited. O is a cause of the production of coarse inclusions
adversely affecting toughness. Therefore, the content of O is 0.005% or less. The
content thereof is preferably 0.003% or less.
[0041] Those described above are fundamental components in the present invention. For the
purposes of improving the strength and toughness of a steel plate, enhancing the hardenability
thereof, and promoting the production of MA, one or more of Cu, Ni, Cr, Mo, V, Ca,
and B may be contained therein as described below.
Cu: 0.5% or less
[0042] Cu need not be added. However, Cu may be added because the addition thereof contributes
to the enhancement of the hardenability of the steel. In order to obtain such an effect,
the addition of 0.05% or more Cu is preferred. However, the addition of more than
0.5% Cu causes the deterioration of toughness. Therefore, in the case of adding Cu,
the content of Cu is preferably 0.5% or less and more preferably 0.4% or less.
Ni: 1% or less
[0043] Ni need not be added. However, Ni may be added because the addition thereof contributes
to the enhancement of the hardenability of the steel and the addition a large amount
thereof does not cause the deterioration of toughness and is effective in strengthening.
In order to obtain such effects, the addition of 0.05% or more Ni is preferred. However,
the content of Ni is preferably 1% or less and more preferably 0.4% or less in the
case of adding Ni because Ni is an expensive element.
Cr: 0.5% or less
[0044] Cr need not be added. However, Cr may be added because Cr, as well as Mn, is an element
effective in obtaining sufficient strength even if the content of C thereof is low.
In order to obtain such an effect, the addition of 0.1% or more Cr is preferred. However,
the excessive addition thereof causes the deterioration of weldability. Therefore,
in the case of adding Cr, the content of Cr is preferably 0.5% or less and more preferably
0.4% or less.
Mo: 0.5% or less
[0045] Mo need not be added. However, Mo may be added because Mo is an element which enhances
the hardenability and which produces MA and strengthens a bainite phase to contribute
to the increase of strength. In order to obtain such effects, the addition of 0.05%
or more Mo is preferred. However, the addition of more than 0.5% Mo causes the deterioration
in toughness of the welded heat affected zone. Therefore, in the case of adding Mo,
the content of Mo is preferably 0.5% or less and more preferably 0.3% or less.
V: 0.1% or less
[0046] V need not be added. However, V may be added because V is an element which enhances
the hardenability and which contributes to the increase of the strength. In order
to obtain such effects, the addition of 0.005% or more V is preferred. However, the
addition of more than 0.1% V causes the deterioration in toughness of the welded heat
affected zone. Therefore, in the case of adding V, the content of V is preferably
0.1% or less and more preferably 0.06% or less.
Ca: 0.0005% to 0.003%
[0047] Ca controls the morphology of sulfide inclusions to improve the toughness and therefore
may be added. When the content thereof is 0.0005% or more, such an effect is developed.
When the content thereof is more than 0.003%, the effect is saturated, the cleanliness
is reduced, and the toughness is deteriorated. Therefore, in the case of adding Ca,
the content of Ca is preferably in the range of 0.0005% to 0.003% and more preferably
0.001% to 0.003%.
B: 0.005% or less
[0048] B may be added because B is an element contributing to the improvement in toughness
of the welded heat affected zone. In order to obtain such an effect, the addition
of 0.0005% or more B is preferred. However, the addition of more than 0.005% B causes
the deterioration of weldability. Therefore, in the case of adding B, the content
of B is preferably 0.005% or less and more preferably 0.003% or less.
[0049] The optimization of the ratio Ti/N that is the ratio of the content of Ti to the
content of N allows the coarsening of austenite in the welded heat affected zone to
be suppressed due to TiN grains and allows the welded heat affected zone to have good
toughness. Therefore, the ratio Ti/N is preferably within the range of 2 to 8 and
more preferably 2 to 5.
[0050] The remainder, other than the above components of the steel plate according to the
present invention, is Fe and unavoidable impurities. It is not denied that an element
other than those described above may be contained therein, unless advantageous effects
of the present invention are impaired. From the viewpoint of the improvement of toughness,
for example, 0.02% or less Mg and/or 0.02% or less of a REM (rare-earth metal) may
be contained therein.
[0051] metallographic microstructure according to the present invention is described below.
2. Metallographic microstructure
[0052] In the present invention, the metallographic microstructure uniformly contains bainite,
which is a main phase, and M-A constituent (MA) having a area fraction of 3% to 20%
and an equivalent circle diameter of 3.0 µm or less. The term "main phase" as used
herein refers to a phase with a area fraction of 80% or more.
[0053] The steel plate has a two-phase microstructure consisting of bainite and MA uniformly
produced therein, that is, a composite microstructure containing soft tempered bainite
and hard MA and therefore has low yield ratio and high uniform elongation. In the
composite microstructure, which contains soft tempered bainite and hard MA, a soft
phase is responsible for deformation and therefore a high uniform elongation of 7%
or more can be achieved.
[0054] The percentage of MA in the microstructure is 3% to 20% in terms of the area fraction
(calculated from the average of the percentages of the areas of MA in arbitrary cross
sections of the steel plate in the rolling direction thereof, the thickness direction
thereof, and the like) of MA. An MA area fraction of less than 3% is insufficient
to achieve low yield ratio and high uniform elongation in some cases and an MA area
fraction of more than 20% causes the deterioration in toughness of the base material
in some cases.
[0055] From the viewpoint of the reduction of yield ratio and the increase of uniform elongation,
the area fraction of MA is preferably 5% to 12%. Fig. 1 shows the relationship between
the area fraction of MA and the uniform elongation of base materials. It is difficult
to achieve a uniform elongation of 7% or more when the area fraction of MA is less
than 3%. Fig. 2 shows the relationship between the area fraction of MA and the yield
ratio of base materials. It is difficult to achieve a yield ratio of 85% or less when
the area fraction of MA is less than 3%.
The area fraction of MA can be calculated from the average of the percentages of the
areas of MA in microstructure photographs of at least four fields or more of view,
the photographs being obtained by, for example, SEM (scanning electron microscope)
observation and being subjected to image processing.
[0056] From the viewpoint of ensuring the toughness of the base material, the equivalent
circle diameter of MA is 3.0 µm or less. Fig. 3 shows the relationship between the
equivalent circle diameter of MA and the toughness of base materials. It is difficult
to adjust the Charpy absorbed energy of a base material to 200 J or more at -20°C
when the equivalent circle diameter of MA. is less than 3.0 µm.
The equivalent circle diameter of MA can be determined in such a manner that a microstructure
photograph obtained by SEM observation is subjected to image processing and the diameters
of circles equal in area to individual MA grains are determined and are then averaged.
[0057] In the present invention, in order to produce MA without adding a large amount of
an expensive alloying element such as Cu, Ni, or Mo, it is important that non-transformed
austenite is stabilized by the addition of Mn and Si and pearlitic transformation
and cementite precipitation are suppressed during reheating and air cooling subsequent
thereto.
From the viewpoint of suppressing ferrite precipitation, the initial cooling temperature
is preferably not lower than the Ar
3 transformation temperature.
[0058] In the present invention, the mechanism of MA production is as described below. Detailed
manufacturing conditions are described below.
[0059] After a slab is heated, rolling is finished in the austenite region and accelerated
cooling is started at the Ar
3 transformation temperature or higher.
[0060] In the following process, the change of the microstructure is as described below:
a manufacturing process in which accelerated cooling is finished during bainite transformation,
that is, in a temperature range in which non-transformed austenite is present, reheating
is performed at a temperature higher than the finish temperature (Bf point) of bainite
transformation, and cooling is then performed.
[0061] The microstructure contains bainite and non-transformed austenite at the end of accelerated
cooling. Reheating is performed at a temperature higher than the Bf point, whereby
non-transformed austenite is transformed into bainite. Since the amount of solid solution
of carbon in bainite produced at such a relatively high temperature is small, C is
emitted into surrounding non-transformed austenite.
[0062] Therefore, the amount of C in non-transformed austenite increases as bainite transformation
proceeds during reheating. When certain amounts of Mn, Si, and the like, which are
austenite-stabilizing elements, are contained, non-transformed austenite in which
C is concentrated remains at the end of reheating and is then transformed into MA
during cooling subsequent to reheating. The microstructure finally contains bainite
and MA produced therein.
[0063] In the present invention, it is important that reheating is performed subsequently
to accelerated cooling in a temperature range in which non-transformed austenite is
present. When the initial reheating temperature is not higher than the Bf point, bainite
transformation is completed and non-transformed austenite is not present. Therefore,
the initial reheating temperature needs to be higher than the Bf point.
[0064] Cooling subsequent to reheating does not affect the transformation of MA, therefore
is not particularly limited, and is preferably air cooling principally. In the present
invention, steel containing certain amounts of Mn and Si is used, accelerated cooling
is stopped during bainite transformation, and continuous reheating is immediately
performed, whereby hard MA can be produced without reducing manufacturing efficiency.
[0065] The steel according to the present invention has the metallographic microstructure,
which uniformly contains bainite, which is a main phase, and a certain amount of MA.
Those containing a microstructure other than bainite and MA or a precipitate are included
in the scope of the present invention unless advantageous effects of the present invention
are impaired.
[0066] In particular, when one or more of ferrite (particularly polygonal ferrite), pearlite,
cementite, and the like coexist, the strength is reduced. However, when the area fraction
of a microstructure other than bainite and MA is small, a reduction in strength is
negligible. Therefore, a metallographic microstructure other than bainite and MA,
that is, one or more of ferrite, pearlite, cementite, and the like may be contained
when the total area fraction thereof in the microstructure is 3% or less.
[0067] The above-mentioned metallographic microstructure can be obtained in such a manner
that the steel having the above-mentioned composition is manufactured by a method
below.
3. Manufacturing conditions
[0068] It is preferred that the steel having the above-mentioned composition is produced
in a production unit such as a steel converter or an electric furnace in accordance
with common practice and is then processed into a steel material such as a slab by
continuous casting or ingot casting-blooming in accordance with common practice. A
production process and a casting process are not limited to the above processes. The
steel material is rolled so as to have desired properties and a desired shape, is
cooled subsequently to rolling, and is then heated.
[0069] In the present invention, each of temperatures such as the heating temperature, the
finishing rolling temperature, the finishing cooling temperature, and the reheating
temperature is the average temperature of the steel plate. The average temperature
thereof is determined from the surface temperature of a slab or the steel plate by
calculation in consideration of a parameter such as thickness or thermal conductivity.
The cooling rate is the average obtained by dividing the temperature difference required
for cooling to a finishing cooling temperature (500°C to 680°C) by the time taken
to perform cooling after hot rolling is finished.
[0070] The heating rate is the average obtained by dividing the temperature difference required
for reheating to a reheating temperature (550°C to 750°C) by the time taken to perform
reheating after cooling. Manufacturing conditions are described below in detail.
[0071] The Ar
3 transformation temperature used is a value calculated by the following equation:

Heating temperature: 1000°C to 1300°C
[0072] When the heating temperature is lower than 1000°C, the solid solution of carbides
is insufficient and required strength cannot be achieved. When the heating temperature
is higher than 1300°C, the toughness of the base material is deteriorated. Therefore,
the heating temperature is within the range of 1000°C to 1300°C.
Finishing rolling temperature: not lower than Ar3 transformation temperature
[0073] When the finishing rolling temperature is lower than the Ar
3 transformation temperature, the concentration of C in non-transformed austenite is
insufficient during reheating and therefore MA is not produced because the transformation
rate of ferrite is reduced. Therefore, the finishing rolling temperature is not lower
than the Ar
3 transformation temperature.
Accumulative rolling reduction at 900°C or lower: 50% or more
[0074] This condition is one of important manufacturing conditions. A temperature range
not higher than 900°C corresponds to the no-recrystallization temperature range in
austenite. When the accumulative rolling reduction in this temperature range is 50%
or more, austenite grains can be refined and therefore the number of sites producing
MA at prior austenite grain boundaries is increased, which contributes to suppressing
the coarsening of MA.
[0075] When the accumulative rolling reduction at 900°C or lower is less than 50%, the uniform
elongation is reduced or the toughness of the base material is reduced in some cases
because the equivalent circle diameter of produced MA exceeds 3.0 µm. Therefore, the
accumulative rolling reduction at 900°C or lower is 50% or more.
Cooling rate and finishing cooling temperature: 5 °C/s or more and 500°C to 680°C,
respectively
[0076] Accelerated cooling is performed immediately after rolling is finished. In the case
where the initial cooling temperature is not higher than the Ar
3 transformation temperature and therefore polygonal ferrite is produced, a reduction
in strength is caused and MA is unlikely to be produced. Therefore, the initial cooling
temperature is preferably not lower than the Ar
3 transformation temperature.
[0077] The cooling rate is 5 °C/s or more. When the cooling rate is less than 5 °C/s, pearlite
is produced during cooling and therefore sufficient strength or low yield ratio cannot
be achieved. Therefore, the cooling rate after rolling is 5 °C/s or more.
[0078] In the present invention, supercooling is performed to a bainite transformation region
by accelerated cooling, whereby bainite transformation can be completed during reheating
without temperature maintenance during reheating.
[0079] The finishing cooling temperature is 500°C to 680°C. In the present invention, this
process is an important manufacturing condition. In the present invention, non-transformed
austenite which is present after reheating and in which C is concentrated is transformed
into MA during air cooling.
[0080] That is, cooling needs to be finished in a temperature range in which non-transformed
austenite that is being transformed into bainite is present. When the finishing cooling
temperature is lower than 500°C, bainite transformation is completed; hence, MA is
not produced during cooling and therefore low yield ratio cannot be achieved. When
the finishing cooling temperature is higher than 680°C, C is consumed by pearlite
precipitated during cooling and therefore MA is not produced. Therefore, the finishing
cooling temperature is 500°C to 680°C. In order to ensure the area fraction of MA
that is preferable in achieving better strength and toughness, the finishing cooling
temperature is preferably 550°C to 660°C. An arbitrary cooling system can be used
for accelerated cooling.
[0081] Heating rate after accelerated cooling and reheating temperature: 2.0 °C/s or more
and 550°C to 750°C, respectively
Reheating is performed to a temperature of 550°C to 750°C at a heating rate of 2.0
°C/s or more immediately after accelerated cooling is finished. The expression "reheating
is performed immediately after accelerated cooling is finished" as used herein means
that reheating is performed a heating rate of 2.0 °C/s or more within 120 seconds
after accelerated cooling is finished.
[0082] In the present invention, this process is also an important manufacturing condition.
Non-transformed austenite is transformed into bainite during reheating subsequent
to accelerated cooling as described above and therefore C is emitted into remaining
non-transformed austenite. The non-transformed austenite in which C is concentrated
is transformed into MA during air cooling subsequent to reheating.
[0083] In order to obtain MA, reheating needs to be performed from a temperature not lower
than the Bf point to a temperature of 550°C to 750°C after accelerated cooling.
[0084] When the heating rate is less than 2.0 °C/s, it takes a long time to achieve a target
heating temperature and therefore manufacturing efficiency is low. Furthermore, the
coarsening of MA is caused in some cases and low yield ratio or sufficient uniform
elongation cannot be achieved. This mechanism is not necessarily clear but is believed
to be that the coarsening of a C-concentrated region and the coarsening of MA produced
during cooling subsequent to reheating are suppressed by increasing the heating rate
during reheating to 2.0 °C/s or more.
[0085] When the reheating temperature is lower than 550°C, bainite transformation does not
occur sufficiently and the emission of C into non-transformed austenite is insufficient;
hence, MA is not produced and low yield ratio cannot be achieved. When the reheating
temperature is higher than 750°C, sufficient strength cannot be achieved because of
the softening of bainite. Therefore, the reheating temperature is within the range
of 550°C to 750°C.
[0086] In the present invention, it is important to perform reheating subsequent to accelerated
cooling from a temperature range in which non-transformed austenite is present. When
the initial reheating temperature is not higher than the Bf point, bainite transformation
is completed and therefore non-transformed austenite is not present. Therefore, the
initial reheating temperature needs to be higher than the Bf point.
In order to securely concentrate C, which is being transformed into bainite, in non-transformed
austenite, the temperature is preferably increased from the initial reheating temperature
by 50°C or more. The time to maintain the initial reheating temperature need not be
particularly set.
[0087] Since MA is sufficiently obtained by a manufacturing method according to the present
invention even if cooling is performed immediately after reheating, low yield ratio
and high uniform elongation can be achieved. However, in order to promote the diffusion
of C to ensure the area fraction of MA, temperature maintenance may be performed for
30 minutes or less during reheating. If temperature maintenance is performed for more
than 30 minutes, then recovery occurs in a bainite phase to cause a reduction in strength
in some cases.
Basically, the rate of cooling subsequent to reheating is preferably equal to the
rate of air cooling.
[0088] In order to perform reheating subsequently to accelerated cooling, a heater may be
placed downstream of a cooling system for performing accelerated cooling. The heater
used is preferably a gas burner furnace or induction heating apparatus capable of
rapidly heating the steel plate.
[0089] As described above, in the present invention, the number of the MA-producing sites
can be increased and MA can be uniformly and finely dispersed through the refining
of the austenite grains by applying an accumulative rolling reduction of 50% or more
in a no-recrystallization temperature range in austenite not higher than 900°C. Furthermore,
in the present invention, since the coarsening of MA is suppressed by increasing the
heating rate during reheating subsequent to accelerated cooling, the equivalent circle
diameter of MA can be reduced to 3.0 µm or less. This allows the uniform elongation
to be increased to 7% or more as compared with conventional products while a low yield
ratio of 85% or less and good low-temperature toughness are maintained.
[0090] Furthermore, the decomposition of MA in the steel according to the present invention
is slight and a predetermined metallographic microstructure that is a two-phase microstructure
consisting of bainite and MA can be maintained even if the steel suffers such a thermal
history that deteriorates properties of conventional steels because of strain ageing.
As a result, in the present invention, an increase in yield strength (YS) due to strain
ageing, an increase in yield ratio due thereto, and a reduction in uniform elongation
can be suppressed even through a thermal history corresponding to heating at 250°C
for 30 minutes, that is, heating at high temperature for a long time in a coating
process for common steel pipes. In the steel according to the present invention, a
yield ratio of 85% or less and a uniform elongation of 7% or more can be ensured even
if the steel suffers such a thermal history that deteriorates properties of conventional
steels because of strain ageing.
[Example 1]
[0091] Steels (Steels A to J) having compositions shown in Table 1 were processed into slabs
by continuous casting and steel plates (Nos. 1 to 16) with a thickness of 20 mm or
33 mm were manufactured from the slabs.
[0092] Each heated slab was hot-rolled, was immediately cooled in an accelerated cooling
system of a water-cooled type, and was then reheated in an induction heating furnace
or a gas burner furnace. The induction heating furnace and the accelerated cooling
system were arranged on the same line.
[0093] Conditions for manufacturing the steel plates (Nos. 1 to 16) are shown in Table 2.
Temperatures such as the heating temperature, the finishing rolling temperature, the
final (finishing) cooling temperature, and the reheating temperature were the average
temperatures of the steel plates. The average temperature was determined from the
surface temperature of each slab or steel plate by calculation using a parameter such
as thickness or thermal conductivity.
[0094] The cooling rate is the average obtained by dividing the temperature difference required
for cooling to a final (finishing) cooling temperature (460°C to 630°C) by the time
taken to perform cooling after hot rolling is finished. The reheating rate (heating
rate) is the average obtained by dividing the temperature difference required for
reheating to a reheating temperature (540°C to 680°C) by the time taken to perform
reheating after cooling.
[0095] The steel plates manufactured as described above were measured for mechanical property.
The measurement results are shown in Table 3. The tensile strength was evaluated in
such a manner that two tension test specimens were taken from each steel plate in
a direction perpendicular to the rolling direction thereof so as to have the same
thickness as that of the steel plate and were subjected to a tension test and the
average was determined.
[0096] A tensile strength of 517 MPa or more (API 5L X60 or higher) was defined as the strength
required in the present invention. The yield ratio and the uniform elongation were
each evaluated in such a manner that two tension test specimens were taken from the
steel plate in the rolling direction thereof so as to have the same thickness as that
of the steel plate and were subjected to a tension test and the average was determined.
A yield ratio of 85% or less and a uniform elongation of 7% or more were deformation
properties required in the present invention.
[0097] For the toughness of each base material, three full-size Charpy V-notch specimens
were taken from the steel plate in a direction perpendicular to the rolling direction,
were subjected to a Charpy test, and were measured for absorbed energy at -20°C and
the average thereof was determined. Those having an absorbed energy of 200 J or more
at -20°C were judged to be good.
[0098] For the toughness of each welded heat affected zone (HAZ), three specimens to which
a thermal history corresponding to a heat input of 40 kJ/cm was applied with a reproducing
apparatus of weld thermal cycles were taken and were subjected to a Charpy impact
test. These specimens were measured for absorbed energy at -20°C and the average thereof
was determined. Those having an absorbed energy of 100 J or more at -20°C were judged
to be good.
[0099] After the manufactured steel plates were subjected to strain ageing treatment by
maintaining the steel plates at 250°C for 30 minutes, the base materials were subjected
to the tension test and the Charpy impact test and the welded heat affected zones
(HAZ) were also subjected to the Charpy impact test, followed by evaluation. Evaluation
standards after strain ageing treatment were the same as the above-mentioned evaluation
standards before strain ageing treatment.
[0100] As shown in Table 3, the compositions and manufacturing methods of Nos. 1 to 7, which
are examples of the present invention, are within the scope of the present invention;
Nos. 1 to 7 have a high tensile strength of 517 MPa or more, a low yield ratio of
85% or less, and a high uniform elongation of 7% or more before and after strain ageing
treatment at 250°C for 30 minutes; and the base materials and the welded heat affected
zones have good toughness.
[0101] The steel plates had a microstructure containing bainite and MA produced therein.
MA had a area fraction of 3% to 20%. The area fraction of MA was determined from the
microstructure observed with a scanning electron microscope (SEM) by image processing.
[0102] The compositions of Nos. 8 to 13, which are examples of the present invention, are
within the scope of the present invention and manufacturing methods thereof are outside
the scope of the present invention. Therefore, the area fraction or equivalent circle
diameter of MA in the microstructure of each steel plate is outside the scope of the
present invention. The yield ratio or the uniform elongation is insufficient or good
strength or toughness is not achieved before or after strain ageing treatment at 250°C
for 30 minutes. The compositions of Nos. 14 to 16 are outside the scope of the present
invention. Therefore, the yield ratio and uniform elongation of Nos. 14 and 15 are
outside the scope of the present invention and the toughness of No. 16 is poor.
[Table 1]
[0103]
Table 2
No. |
Steel type |
Plate thickness |
Heating temperature |
Accumulative rolling reduction at 900°C or lower |
Finishing rolling temperature |
Initial cooling temperature |
Cooling rate |
Final cooling temperature |
Reheating unit |
Reheating rate |
Reheating temperature |
Remarks |
|
|
(mm) |
(°C) |
(%) |
(°C) |
(°C) |
(°C/s) |
(°C) |
|
(°C/s) |
(°C) |
|
1 |
A |
33 |
1250 |
75 |
860 |
780 |
20 |
590 |
Induction heating furnace |
2 |
650 |
Examples |
2 |
B |
20 |
1080 |
75 |
850 |
790 |
35 |
620 |
Induction heating furnace |
5 |
650 |
3 |
C |
33 |
1280 |
70 |
840 |
810 |
15 |
540 |
Induction heating furnace |
2 |
680 |
4 |
D |
20 |
1180 |
75 |
820 |
800 |
40 |
600 |
Induction heating furnace |
3 |
650 |
5 |
E |
20 |
1050 |
60 |
840 |
810 |
35 |
630 |
Gas burner furnace |
3 |
680 |
6 |
F |
20 |
1180 |
50 |
850 |
800 |
40 |
610 |
Induction heating furnace |
3 |
660 |
7 |
G |
20 |
1190 |
75 |
870 |
820 |
35 |
570 |
Induction heating furnace |
5 |
650 |
8 |
D |
20 |
950 |
75 |
850 |
790 |
35 |
610 |
induction heating furnace |
7 |
680 |
Comparative Examples |
9 |
D |
20 |
1150 |
45 |
890 |
820 |
35 |
580 |
Induction heating furnace |
8 |
650 |
10 |
D |
20 |
1180 |
75 |
860 |
800 |
3 |
600 |
Induction heating furnace |
8 |
680 |
11 |
E |
20 |
1100 |
65 |
860 |
810 |
30 |
460 |
Induction heating furnace |
3 |
650 |
12 |
E |
20 |
1200 |
75 |
870 |
800 |
35 |
620 |
Induction heating furnace |
0.3 |
680 |
13 |
F |
20 |
1080 |
70 |
820 |
780 |
40 |
510 |
Induction heating furnace |
7 |
540 |
14 |
H |
20 |
1150 |
75 |
860 |
800 |
35 |
610 |
Induction heating furnace |
9 |
650 |
15 |
I |
20 |
1200 |
75 |
820 |
790 |
40 |
550 |
Induction heating furnace |
9 |
680 |
16 |
J |
20 |
1180 |
75 |
820 |
790 |
35 |
580 |
Induction heating furnace |
2 |
650 |
* Underlined values are outside the scope of the present invention. |
Table 3
|
|
|
|
|
Before ageing treatment at 250°C for 30 minute. |
After ageing treatment at 250°C for 30 minute |
No. |
Steel type |
Plate thickness |
Volume fraction of MA in microstructure of steel plate |
Equivalent circle diameter of MA in steel plate |
Tensile strength |
Yield ratio |
Uniform elongation |
Base material toughness vE-20°C |
HAZ toughness vE-20°C |
Tensile strength |
Yield ratio |
Uniform elongation |
Base material toughness vE-20°C |
HAZ toughness vE-20°C |
Remarks |
|
|
(mm) |
(%) |
(µm) |
(MPa) |
(%) |
(%) |
(J) |
(J) |
(MPa) |
(%) |
(%) |
(J) |
(J) |
|
1 |
A |
33 |
12 |
1.8 |
610 |
78 |
10 |
312 |
131 |
600 |
79 |
10 |
304 |
122 |
Examples |
2 |
B |
20 |
10 |
1.4 |
557 |
77 |
10 |
322 |
144 |
566 |
79 |
10 |
302 |
133 |
3 |
C |
33 |
15 |
2.8 |
677 |
71 |
8.8 |
234 |
106 |
655 |
74 |
9.0 |
245 |
115 |
4 |
D |
20 |
9 |
1 6 |
624 |
73 |
11 |
284 |
166 |
616 |
74 |
10 |
292 |
125 |
5 |
E |
20 |
8 |
1.8 |
633 |
81 |
10 |
318 |
159 |
621 |
82 |
10 |
294 |
121 |
6 |
F |
20 |
11 |
1.2 |
574 |
70 |
12 |
353 |
148 |
547 |
73 |
11 |
342 |
155 |
7 |
G |
20 |
5 |
1.4 |
533 |
75 |
11 |
365 |
172 |
528 |
76 |
11 |
341 |
164 |
8 |
D |
20 |
2 |
2.5 |
502 |
87 |
60 |
355 |
188 |
510 |
86 |
67 |
341 |
175 |
Comparative Examples |
9 |
D |
20 |
8 |
3 5 |
600 |
77 |
11 |
166 |
137 |
604 |
78 |
10 |
174 |
124 |
10 |
D |
20 |
2 |
2.4 |
590 |
85 |
10 |
267 |
135 |
588 |
86 |
9.1 |
255 |
130 |
11 |
E |
20 |
1 |
1.5 |
540 |
92 |
62 |
285 |
165 |
541 |
91 |
52 |
277 |
156 |
12 |
E |
20 |
1 |
1.6 |
660 |
83 |
6.8 |
288 |
181 |
642 |
84 |
66 |
301 |
156 |
13 |
F |
20 |
0 |
1.3 |
660 |
89 |
60 |
312 |
112 |
647 |
88 |
63 |
304 |
105 |
14 |
H |
20 |
1 |
1.4 |
655 |
90 |
5.6 |
253 |
148 |
644 |
89 |
64 |
244 |
152 |
15 |
I |
20 |
2 |
1.8 |
623 |
91 |
60 |
221 |
155 |
630 |
90 |
6.5 |
214 |
123 |
16 |
J |
20 |
18 |
4.3 |
680 |
66 |
10 |
202 |
13 |
674 |
69 |
8.8 |
222 |
16 |
* Underlined values are outside the scope of the present invention. |